Isopropyl Rubbing Alcohol 99% Liquid
FDA Label NDC 52000-049

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Isopropyl Rubbing Alcohol 99% (NDC 52000-049). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients (by volume)

Isopropyl alcohol (99% conc.)

Otc - Purpose

Purpose

First aid antiseptic

Indications & Usage

Uses

  • first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

Warnings

For external use only; flammable, keep away from fire or flame, heat, spark, electrical

Otc - Ask Doctor

Ask a doctor before use if you have

  • deep punctured wounds, animal bites or serious burns

Otc - When Using

When using this product

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor

Otc - Stop Use

Stop using this product if

  • condition persists or gets worse

Otc - Keep Out Of Reach Of Children

Keep this and all drugs out of the reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

Dosage & Administration

Directions

  • clean effected area
  • apply small amount of this product on the area 1-3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other

Other information

  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • will produce serious gastric disturbances if taken internally

Inactive Ingredient

Inactive Ingredient

Purified Water

Package Label.Principal Display Panel

PRINCIPAL DISPLAY PANEL

ISOPROPYL RUBBING ALCOHOL 99%
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)

Label (Isopropyl Rubbing Alcohol 99)

Label (Isopropyl Rubbing Alcohol 99)

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